×
×
PubCaseFinder
About
Datasets
History
Terms
RDF
API
Contact
EN
/
JA
Wilson disease
Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.
Edema
An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body.
Total:
0
20
40
60
100
(per page)
PMID (PMCID)